Evidence map›Paper›PMID 39013087›Full record

ArticleMagyar onkologia2024

[Mutation frequency of homologous recombination repair genes in prostate adenocarcinomas].

Zsombor Melegh, Erzsébet Csernák, Andrea Kohánka, Mónika Rubovszkyné Gallai, Eszter Bencze, Melinda Szőke, Luca Pap, Andrea Simon, Zsófia Küronya, Krisztina Biró and 2 more

Abstract readEnglish Abstract
In one paragraph

Article in Magyar onkologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Zsombor MeleghSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Erzsébet CsernákSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Andrea KohánkaSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Mónika Rubovszkyné GallaiSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Eszter BenczeSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Melinda SzőkeSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Luca PapSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Andrea SimonSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Zsófia KüronyaGyógyszerterápiás Központ, Urogenitális Tumorok és Klinikai Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.
Krisztina BiróGyógyszerterápiás Központ, Urogenitális Tumorok és Klinikai Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.
Lajos GécziNemzeti Tumorbiológiai Laboratórium, Országos Onkológiai Intézet, Budapest, Hungary.
Erika TóthSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The best predictive marker for the expected efficacy of PARP inhibitor therapy is mutations in BRCA1/2 or other homologous recombination repair genes. These tests are part of routine molecular pathology diagnostics. Among 281 patients with prostate adenocarcinoma, somatic pathogenic mutations in one of these genes were identified in 21.4% of patients. In 28.5% of the patients, the test was unsuccessful; the main limitation of successful testing was the age of the paraffin blocks and low DNA concentration. In the case of BRCA1/2 testing, the success rate was significantly reduced for samples older than 5 years, while in tests involving a broader set of homologous recombination repair genes, the success rate was significantly reduced for samples older than 2 years. Therefore, it is very important to test high-risk prostate cancers at the time of primary diagnosis, and probably also liquid biopsy testing of circulating tumor DNA will play an important role in safe diagnosis in the near future.

Indexed as

AdenocarcinomaProstatic NeoplasmsRecombinational DNA RepairAgedBiomarkers, TumorBRCA1 ProteinBRCA2 ProteinHumansMaleMiddle AgedMutationMutation RatePoly(ADP-ribose) Polymerase InhibitorsBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID39013087
PMCPMC11870680

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.